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439157002: Hereditary combined coagulation factor deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2787558013 Hereditary combined coagulation factor deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2795244014 Hereditary combined coagulation factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary combined coagulation factor deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Hereditary combined coagulation factor deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Hereditary combined coagulation factor deficiency (disorder) est un(e) (attribut) Hereditary coagulation factor deficiency true Inferred relationship Some
Hereditary combined coagulation factor deficiency (disorder) est un(e) (attribut) Combined coagulation factor deficiency true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
déficit combiné en facteurs V et VIII est un(e) (attribut) True Hereditary combined coagulation factor deficiency (disorder) Inferred relationship Some
Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) est un(e) (attribut) True Hereditary combined coagulation factor deficiency (disorder) Inferred relationship Some

This concept is not in any reference sets

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